Disease #07153 (DEHMBA (developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities), OMIM:619595)

Official abbreviation	DEHMBA
Name	developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities
OMIM ID	619595
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SRCAP
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-02-22 10:55:57 +01:00 (CET)
Date last edited	N/A

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Global Variome shared LOVD